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07:11Two pure-breeding wheat strains, one producing dark red kernels and the other producing white kernels, are crossed to produce F₁ with pink kernel color. When an F₁ plant is self-fertilized and its seed collected and planted, the resulting F₂ consists of 160 plants with kernel colors as shown in the following table.
If an F₁ plant is crossed to a dark red plant, what are the expected progeny phenotypes, and what is the expected proportion of each phenotype?
In studies of human MZ and DZ twin pairs of the same sex who are reared together, the following concordance values are identified for various traits. Based on the values shown, describe the relative importance of genes versus the influence of environmental factors for each trait.
During a visit, your grandparents comment on how tall you are compared with them. You tell them that in your genetics class, you learned that height in humans has high heritability, although environmental factors also influence adult height. You correctly explain the meaning of heritability, and your grandfather asks, 'How can height be highly heritable and still be influenced by the environment?' What explanation do you give your grandfather?
Applied to the study of the human genome, a goal of GWAS is to locate chromosome regions that are likely to contain genes influencing the risk of disease. Specific genes can be identified in these regions, and particular mutant alleles that increase disease risk can be sequenced. To date, the identification of alleles that increase disease risk has occasionally led to a new therapeutic strategy, but more often the identification of disease alleles is the only outcome.
From a physician's point of view, what is the value of being able to identify alleles that increase the risk of a particular disease?
Applied to the study of the human genome, a goal of GWAS is to locate chromosome regions that are likely to contain genes influencing the risk of disease. Specific genes can be identified in these regions, and particular mutant alleles that increase disease risk can be sequenced. To date, the identification of alleles that increase disease risk has occasionally led to a new therapeutic strategy, but more often the identification of disease alleles is the only outcome.
What is the value of being able to identify alleles that increase disease risk for a person who is currently free of the disease but who is at risk of developing the disease due to its presence in the family?
Applied to the study of the human genome, a goal of GWAS is to locate chromosome regions that are likely to contain genes influencing the risk of disease. Specific genes can be identified in these regions, and particular mutant alleles that increase disease risk can be sequenced. To date, the identification of alleles that increase disease risk has occasionally led to a new therapeutic strategy, but more often the identification of disease alleles is the only outcome.
What personal or ethical issues arising from GWAS might be of concern to physicians or to those who might carry an allele that increases disease risk?
